(Q52014584)

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Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

congenital heart disease

1 reference

based on heuristic

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David A Elliott

1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

2

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Richard P. Harvey

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Richard P Harvey

12

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7

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Paul Grossfeld

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

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Thomas Yeoh

3

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Suchitra Chandar

4

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Fiona McKenzie

5

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Peter Taylor

6

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Diane Fatkin

8

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Owen Jones

9

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Peter Hayes

10

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Michael Feneley

11

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

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publication date

1 June 2003

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Journal of the American College of Cardiology

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

41

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Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

11

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

2072-2076

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital heart disease caused by mutations in the transcription factor NKX2-5

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel point mutation in the cardiac transcription factor CSX/NKX2.5 associated with congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

NKX2.5 mutations in patients with tetralogy of fallot

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac septal and valvular dysmorphogenesis in mice heterozygous for mutations in the homeobox gene Nkx2-5

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of connexin43 (alpha1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE).

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

The association between the diameter of a patent foramen ovale and the risk of embolic cerebrovascular events

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Reduced penetrance, variable expressivity, and genetic heterogeneity of familial atrial septal defects

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Homeodomain factor Nkx2-5 controls left/right asymmetric expression of bHLH gene eHand during murine heart development

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2803%2900420-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0735-1097(03)00420-0

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/12798584

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